Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP92684.RAi0fTrQpovCDy4OisNzS7Liw1q1iHr70i0DGuCo0Xz4c130_assertion description "[Haplotypic diversity in human CEACAM genes: effects on susceptibility to meningococcal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92684.RAi0fTrQpovCDy4OisNzS7Liw1q1iHr70i0DGuCo0Xz4c130_provenance.
- NP92685.RAtYWIyil18v6OHO0sDyT6Wb_lXRAZRJtC3QjEw9jahb0130_assertion description "[Haplotypic diversity in human CEACAM genes: effects on susceptibility to meningococcal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92685.RAtYWIyil18v6OHO0sDyT6Wb_lXRAZRJtC3QjEw9jahb0130_provenance.
- NP92687.RAn2j-bf2o21C_trhEA40vEc3LdlQDc8JGxwDJmUBzDx0130_assertion description "[A new variation in the promoter region, the -604 C>T, and the Leu72Met polymorphism of the ghrelin gene are associated with protection to insulin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92687.RAn2j-bf2o21C_trhEA40vEc3LdlQDc8JGxwDJmUBzDx0130_provenance.
- NP92689.RAtzppkZ7l58hXqJCRwejHeDV9eCYk6TsD4AVU35oSht8130_assertion description "[Association study between Gilles de la Tourette Syndrome and two genes in the Robo-Slit pathway located in the chromosome 11q24 linked/associated region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92689.RAtzppkZ7l58hXqJCRwejHeDV9eCYk6TsD4AVU35oSht8130_provenance.
- NP92695.RAo8g1WVL6RmSNW9ejxsrRQuPjVywc9nuhlTNn_yUvUBg130_assertion description "[E-cadherin gene polymorphisms and haplotype associated with the occurrence of epithelial ovarian cancer in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92695.RAo8g1WVL6RmSNW9ejxsrRQuPjVywc9nuhlTNn_yUvUBg130_provenance.
- NP92696.RAp_21zVuQpZKJq0vXWHUhZfaJfHF_AybVLW3AD77VNOE130_assertion description "[The E-cadherin gene polymorphism 160C->A and cancer risk: A HuGE review and meta-analysis of 26 case-control studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92696.RAp_21zVuQpZKJq0vXWHUhZfaJfHF_AybVLW3AD77VNOE130_provenance.
- NP92697.RAvc00mtBb3LYkdk2CaWCUy00-EHcZ14P2N-Z_97PsoN0130_assertion description "[These results support the hypothesis of a protective effect for the G allele of rs2433320 in the PDLIM5 gene in recurrent MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92697.RAvc00mtBb3LYkdk2CaWCUy00-EHcZ14P2N-Z_97PsoN0130_provenance.
- NP92699.RAgdzUw4trSvheIffH0YPwpZ09tuTbuuR5vLc7T1T6q9Q130_assertion description "[Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92699.RAgdzUw4trSvheIffH0YPwpZ09tuTbuuR5vLc7T1T6q9Q130_provenance.
- NP92702.RAs0W4gN8s4-nvSIW3XjgyrKfl-jpOU_LVvmxTM5xytXI130_assertion description "[A novel Zip2 Gln/Arg/Leu codon 2 polymorphism is associated with carotid artery disease in aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92702.RAs0W4gN8s4-nvSIW3XjgyrKfl-jpOU_LVvmxTM5xytXI130_provenance.
- NP92709.RApZhoJxvsRiIKM5d27RlY4UR6OsJRIw75qZ-N3ZkJ69Q130_assertion description "[Genotype modulators of clinical severity in McArdle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92709.RApZhoJxvsRiIKM5d27RlY4UR6OsJRIw75qZ-N3ZkJ69Q130_provenance.
- NP92710.RAlhhWQvW5q_khRkT4-ruy7BSfRGZNP-OEIMuLlXVsuz8130_assertion description "[Functional BSND variants in essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92710.RAlhhWQvW5q_khRkT4-ruy7BSfRGZNP-OEIMuLlXVsuz8130_provenance.
- NP92713.RAuyRIIKnFkYW4DlBjbzTY2FZ8U4009fk53toJVZMBeOA130_assertion description "[Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92713.RAuyRIIKnFkYW4DlBjbzTY2FZ8U4009fk53toJVZMBeOA130_provenance.
- NP92715.RAgsHOo00gAvcpmQfxiGsUrnQ_6jQJ24X8FRngr-uvqOw130_assertion description "[No association of KIR genes with Behcet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92715.RAgsHOo00gAvcpmQfxiGsUrnQ_6jQJ24X8FRngr-uvqOw130_provenance.
- NP92722.RAozlZ47sDHyLBuHoRQIJPFpNC3Rz8sO5S1_BKKliU11Q130_assertion description "[A polymorphism in CD14 modifies the effect of farm milk consumption on allergic diseases and CD14 gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92722.RAozlZ47sDHyLBuHoRQIJPFpNC3Rz8sO5S1_BKKliU11Q130_provenance.
- NP92727.RAsMc9AXsYQJUmk_R4FVAoW2NE-L8HWb3zPue09xgA0gA130_assertion description "[The allele frequencies between periodontitis patients and the control group for the CCR5-Delta32 mutation were not significantly different (P=0.801).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92727.RAsMc9AXsYQJUmk_R4FVAoW2NE-L8HWb3zPue09xgA0gA130_provenance.
- NP92744.RAp_8bXWAHXDw5Vx-KBP6Mk_tHMoTdYlkRQCHJAqeopUw130_assertion description "[We enrolled 250 Han Chinese in Taiwan screening for the single nucleotide polymorphisms (SNPs) in TLRs associated with viral infection, including TLR2, TLR3, TLR4, TLR7, TLR8, and TLR9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92744.RAp_8bXWAHXDw5Vx-KBP6Mk_tHMoTdYlkRQCHJAqeopUw130_provenance.
- NP92745.RAh3jm7wHEMnACCLpwSc5AUqzHZMofQvMftWOGRxPtcfE130_assertion description "[We enrolled 250 Han Chinese in Taiwan screening for the single nucleotide polymorphisms (SNPs) in TLRs associated with viral infection, including TLR2, TLR3, TLR4, TLR7, TLR8, and TLR9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92745.RAh3jm7wHEMnACCLpwSc5AUqzHZMofQvMftWOGRxPtcfE130_provenance.
- NP92747.RAnoqtmEWy3rH1yJoduyuhCmqvVYfMjilDMHiN8erkWP4130_assertion description "[Our results show that XT-I polymorphisms potentially confer to the genetic susceptibility of AAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92747.RAnoqtmEWy3rH1yJoduyuhCmqvVYfMjilDMHiN8erkWP4130_provenance.
- NP92751.RAudENadd5xv2nk81Ke1s_n43syX5NuK0BaDFjlEawkIU130_assertion description "[Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92751.RAudENadd5xv2nk81Ke1s_n43syX5NuK0BaDFjlEawkIU130_provenance.
- NP92758.RAlbtgImr0C3pVzlTPdWzlNEU0qUpu43pq9ZQVdBjW2iM130_assertion description "[Polymorphisms of interleukin-6, hepatic lipase and calpain-10 genes, and preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92758.RAlbtgImr0C3pVzlTPdWzlNEU0qUpu43pq9ZQVdBjW2iM130_provenance.
- NP92767.RAvgoshlhYiWeWXchjInHc5Xo7nUPj5w2du9ARCUMSc0g130_assertion description "[Our findings suggest that Sotos syndrome is a rare cause of autism spectrum disorders and that screening for NSD1 mutations and deletions in patients with autism and macrocephaly is not warranted in the absence of other features of Sotos syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92767.RAvgoshlhYiWeWXchjInHc5Xo7nUPj5w2du9ARCUMSc0g130_provenance.
- NP92769.RApJoBGgqBN-y20KW0IBpUeUCK-Zt98otDXGlnWNYqJf8130_assertion description "[An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92769.RApJoBGgqBN-y20KW0IBpUeUCK-Zt98otDXGlnWNYqJf8130_provenance.
- NP92770.RAm4VmL9IWz3vYMwmcaWw0nANZNwQEmDmQi55tl5EB8W0130_assertion description "[These results suggest that DOCK9 contributes to both risk and increased illness severity in bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92770.RAm4VmL9IWz3vYMwmcaWw0nANZNwQEmDmQi55tl5EB8W0130_provenance.
- NP92795.RAj2Fg2YawPStBpy6_XfWtZXx4KuT-dCnPb5ktjZL6ViM130_assertion description "[In this study, the XRCC1 1915C allele was associated with a lower SGC risk, and the XRCC1 194Trp allele was associated with a higher SGC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92795.RAj2Fg2YawPStBpy6_XfWtZXx4KuT-dCnPb5ktjZL6ViM130_provenance.
- NP92800.RAgKwTTyI6y_7WBoKVxTsFdwVaT_BSiue-NPXOxLcMavM130_assertion description "[This study suggests that NER gene polymorphisms may correlate with recurrence and patient survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92800.RAgKwTTyI6y_7WBoKVxTsFdwVaT_BSiue-NPXOxLcMavM130_provenance.
- NP92801.RAk2LynrAEAggHnGbxsonHRKdaqgfNxoIeDaSpFrxXF5U130_assertion description "[This study suggests that NER gene polymorphisms may correlate with recurrence and patient survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92801.RAk2LynrAEAggHnGbxsonHRKdaqgfNxoIeDaSpFrxXF5U130_provenance.
- NP92808.RAsRzRovC_05kQfqgOaFYBy447NdXIJtAxFs7nQ5ApBGE130_assertion description "[showed a strong influence of the BsmI polymorphism on survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92808.RAsRzRovC_05kQfqgOaFYBy447NdXIJtAxFs7nQ5ApBGE130_provenance.
- NP92809.RAteHxKXHQTM2_1ux0wZg8vK8vH_4Spmv049bt_SVlYX4130_assertion description "[The VDR BsmI gene polymorphism may predict both Hb level and EPO need in HD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92809.RAteHxKXHQTM2_1ux0wZg8vK8vH_4Spmv049bt_SVlYX4130_provenance.
- NP92814.RAubj7aJp1UHkJ51ivMbacnIU9qiYhHKxtFrAjReLSHTk130_assertion description "[Associations between vitamin D, vitamin D receptor gene and the androgen receptor gene with colon and rectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92814.RAubj7aJp1UHkJ51ivMbacnIU9qiYhHKxtFrAjReLSHTk130_provenance.
- NP92820.RAo6SlROR832y0wggWZrwa9JPReuwLwUyLsfhZkIgVIis130_assertion description "[One hundred and thirty-six Chinese Han people, including 54 T1DM patients and 82 unrelated healthy subjects as control were genotyped by polymerase chain reaction-restriction fragment length polymorphism for three restriction sites in the VDR gene, which were ApaI, TaqI, and BamI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92820.RAo6SlROR832y0wggWZrwa9JPReuwLwUyLsfhZkIgVIis130_provenance.
- NP92825.RAnCkrL-6lwxqp6QbrA4nG67cW-gL2-M9uq2iT5Yj1Qu8130_assertion description "[Vitamin D and oestrogen receptor polymorphisms in developmental dysplasia of the hip and primary protrusio acetabuli--a preliminary study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92825.RAnCkrL-6lwxqp6QbrA4nG67cW-gL2-M9uq2iT5Yj1Qu8130_provenance.
- NP92826.RAoAbzxHe1aBAN9aFBT0O7Lr53elHxsFE_oG1WueiT6KQ130_assertion description "[We analyzed VDR gene FokI, ApaI and TaqI polymorphisms in 51 Turkish familial psoriasis patients (psoriasis vulgaris and psoriatic arthritis) and 100 healthy subjects, and evaluated the correlation between VDR genotypes and calcipotriol response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92826.RAoAbzxHe1aBAN9aFBT0O7Lr53elHxsFE_oG1WueiT6KQ130_provenance.
- NP92827.RAq1qaLsHFVx78GbGfRaqp1LF9lwlbnwCRkmrEChQnkgU130_assertion description "[We investigated whether there was any association between VDR gene polymorphisms (BsmI, ApaI, and TaqI) and alopecia areata (AA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92827.RAq1qaLsHFVx78GbGfRaqp1LF9lwlbnwCRkmrEChQnkgU130_provenance.
- NP92828.RAj4VLquvExtul7ibomfZvdBq0BeoRv7uO6fwLntbZhr8130_assertion description "[Genetic polymorphisms of vitamin D receptor (VDR) in Fabry disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92828.RAj4VLquvExtul7ibomfZvdBq0BeoRv7uO6fwLntbZhr8130_provenance.
- NP92834.RAuIFXAc0V1t706D9moVyiwm2neCT5cAo9CrSLTT0W9zg130_assertion description "[Integrated pharmacogenetic prediction of irinotecan pharmacokinetics and toxicity in patients with advanced non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92834.RAuIFXAc0V1t706D9moVyiwm2neCT5cAo9CrSLTT0W9zg130_provenance.
- NP92836.RAqVoYGGyexEH7vqqh-e3jFaFu_8s5uGD_kfZrxPKuIAE130_assertion description "[Identification of a prevalent functional missense polymorphism in the UGT2B10 gene and its association with UGT2B10 inactivation against tobacco-specific nitrosamines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92836.RAqVoYGGyexEH7vqqh-e3jFaFu_8s5uGD_kfZrxPKuIAE130_provenance.
- NP92841.RAv8o1m76CGDJj8ora_LV4YrEGBAAFqbSUKArh9h_nung130_assertion description "[Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92841.RAv8o1m76CGDJj8ora_LV4YrEGBAAFqbSUKArh9h_nung130_provenance.
- NP92843.RAtJNQiimpL7LeUo4xE-H2lXKVuY9v-Pg6ERUSNi9lrT8130_assertion description "[Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92843.RAtJNQiimpL7LeUo4xE-H2lXKVuY9v-Pg6ERUSNi9lrT8130_provenance.
- NP92844.RAvrj7EOLHDSLJsyKW3NR86X8Sv1kLnJ-fOqcmUj7oq6I130_assertion description "[TREX1 polymorphisms associated with autoantibodies in patients with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92844.RAvrj7EOLHDSLJsyKW3NR86X8Sv1kLnJ-fOqcmUj7oq6I130_provenance.
- NP92853.RAn5tx645JuqSlIuUqJFt-rTrUF5vNrqmTkHvHafbD8Iw130_assertion description "[At the two locus genotype level in Hispanics, the TPH1 rs1799913 variant was found to significantly interact with the TPH2 rs7963720 variant and heroin addiction (P=0.022), and with the TPH2 rs4290270 variant and heroin addiction (P=0.011).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92853.RAn5tx645JuqSlIuUqJFt-rTrUF5vNrqmTkHvHafbD8Iw130_provenance.
- NP92854.RAgRIEnn3yh31vBc9Ztc_6gSYiyUklLpmGAK3g9dMw5uU130_assertion description "[Haplotype structure of TP53 locus in Indian population and possible association with head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92854.RAgRIEnn3yh31vBc9Ztc_6gSYiyUklLpmGAK3g9dMw5uU130_provenance.
- NP92857.RAnEubQ54UMjHaPu6brZqHCOLEfBIX3wikUQmaQTpWfeE130_assertion description "[Role of p53 codon 72 polymorphism in recurrent pregnancy loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92857.RAnEubQ54UMjHaPu6brZqHCOLEfBIX3wikUQmaQTpWfeE130_provenance.
- NP92860.RAhDQFkADLB5nHx2iFKtgSpRIULg92xu3FP2sSqEIwI4M130_assertion description "[Effects of arsenic exposure and genetic polymorphisms of p53, glutathione S-transferase M1, T1, and P1 on the risk of carotid atherosclerosis in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92860.RAhDQFkADLB5nHx2iFKtgSpRIULg92xu3FP2sSqEIwI4M130_provenance.
- NP92862.RAh22K_DK1FoVbeLC75MiaQlk5qo0hXOdmiPLlmYPKse0130_assertion description "[Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92862.RAh22K_DK1FoVbeLC75MiaQlk5qo0hXOdmiPLlmYPKse0130_provenance.
- NP92864.RAiiwDh4bbrE2XAblACtZuzmySVxqGcImAt77JTcg6tUo130_assertion description "[These results do not show a significant role for the tested candidate gene variants and also do not support the hypothesis that a common chromosome 1 defective gene influences both FHM and the more common forms of migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92864.RAiiwDh4bbrE2XAblACtZuzmySVxqGcImAt77JTcg6tUo130_provenance.
- NP92871.RAoNQflzyP_SjxZh913b0r6HQdSyRu75LUt_XvI6Sow9w130_assertion description "[The purpose of this study is to examine whether there is an association between some alleles of TNF genes and chronic sinusitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92871.RAoNQflzyP_SjxZh913b0r6HQdSyRu75LUt_XvI6Sow9w130_provenance.
- NP92875.RAvQOFizmf5Oh_GavGbfLcEbes0lmuam0hbOWHVF-fj7s130_assertion description "[Tumor necrosis factor-alpha promoter polymorphisms and the risk of rejection after liver transplantation: a case control analysis of 210 donor-recipient pairs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92875.RAvQOFizmf5Oh_GavGbfLcEbes0lmuam0hbOWHVF-fj7s130_provenance.
- NP92890.RAushVo5QjrXxNNszc996i_oB3nsr0UnbFiXQlVGXugEk130_assertion description "[Tumor necrosis factor alpha HLA-DRB(1) gene polymorphism and genetic susceptibility to cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92890.RAushVo5QjrXxNNszc996i_oB3nsr0UnbFiXQlVGXugEk130_provenance.
- NP92893.RAqaKX1H9FxA79ghgQhezaXJLjQU9EGBajt1Q3mvcsXRc130_assertion description "[Polymorphisms within the tumor necrosis factor and lymphotoxin-alpha genes and endemic pemphigus foliaceus--are there any associations?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92893.RAqaKX1H9FxA79ghgQhezaXJLjQU9EGBajt1Q3mvcsXRc130_provenance.
- NP92894.RAkPbwPLlmRuWKfyTYdV0QesjVQvLvHv8wol6HHs2L9V0130_assertion description "[Tumour necrosis factor-alpha polymorphism as one of the complex inherited factors in pemphigus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92894.RAkPbwPLlmRuWKfyTYdV0QesjVQvLvHv8wol6HHs2L9V0130_provenance.
- NP92897.RAqRXpU0lCFjBakfQWktiq7t8zSxghaTs96g_40RNJcsQ130_assertion description "[Risk of IPF was significant for heterozygotes for: (i) the TNF-alpha (-308 A) allele (A/G) (odds ratio (OR) 2.9; 95% confidence interval (CI) 1.2-7.2; P = 0.02), (ii) homozygotes (A/A) (OR 13.9; 95%CI 1.2-160; P = 0.04) and (iii) carriage of the allele (A/A + A/G) (OR 4; 95%CI 1.6-10.2; P = 0.003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92897.RAqRXpU0lCFjBakfQWktiq7t8zSxghaTs96g_40RNJcsQ130_provenance.
- NP92898.RAk6JJw7ZjpCjByPefLRzX1GUkkTJMhqY3HYcVCz2j_LY130_assertion description "[Analysis of TNF-alpha promoter polymorphisms in the susceptibility to beryllium hypersensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92898.RAk6JJw7ZjpCjByPefLRzX1GUkkTJMhqY3HYcVCz2j_LY130_provenance.
- NP92902.RArQ59-9ero6sYQ6ifpxYm2rUS3mbZzfUSGGfAH5APbOM130_assertion description "[Association of tumor necrosis factor-alpha polymorphisms and ozone-induced change in lung function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92902.RArQ59-9ero6sYQ6ifpxYm2rUS3mbZzfUSGGfAH5APbOM130_provenance.
- NP92904.RAof3GEdQOT-dRkVO7n3-hehFDL0LDwF9gs-th_3k74GY130_assertion description "[Influence of a tumor necrosis factor gene polymorphism in Japanese patients with multiple system atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92904.RAof3GEdQOT-dRkVO7n3-hehFDL0LDwF9gs-th_3k74GY130_provenance.
- NP92905.RAosKuQJ4itqC10PdkdH4zngPk8C35fZDwBDRAFrZZgdQ130_assertion description "[This study aimed to determine whether single nucleotide polymorphisms (SNPs) within tumour necrosis factor-alpha (TNF) and interleukin-10 (IL10) promoters and genes are associated with human African trypanosomiasis (HAT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92905.RAosKuQJ4itqC10PdkdH4zngPk8C35fZDwBDRAFrZZgdQ130_provenance.
- NP92906.RAhZUhxE0oZp_770GpLIWmwyvmCIZE7Q9tzr7MKW2FDeo130_assertion description "[TNF-alpha G-308A polymorphism is associated with rheumatic fever and correlates with increased TNF-alpha production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92906.RAhZUhxE0oZp_770GpLIWmwyvmCIZE7Q9tzr7MKW2FDeo130_provenance.
- NP92916.RAqWKswM9l3dPqXbdETzpAlOVT3WiKdtaufv2CKN9prhw130_assertion description "[In our study, we aimed to investigate the association between these three cytokines' single nucleotide polymorphisms (IL-6 gene G(-174)C, TNF-alpha gene G(-308)A and IL-1beta gene C(3954)T polymorphisms) and age-at-onset of type 1 diabetes mellitus (T1DM) in 165 diabetic children (median age: 17 years).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92916.RAqWKswM9l3dPqXbdETzpAlOVT3WiKdtaufv2CKN9prhw130_provenance.
- NP92917.RAinGkUSOrgOexUR_Pk0g5xfb_FyNwUbrXrjFkJVM1pwM130_assertion description "[Associations of TNF-A-1031TT and -857TT genotypes with Helicobacter pylori seropositivity and gastric atrophy among Japanese Brazilians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92917.RAinGkUSOrgOexUR_Pk0g5xfb_FyNwUbrXrjFkJVM1pwM130_provenance.
- NP92919.RAhyiS0mfZF_U_ILqr_dtrpS95fA2KumilN4QxtBZyqz0130_assertion description "[Cytokine gene polymorphisms involved in chronicity and complications of anterior uveitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92919.RAhyiS0mfZF_U_ILqr_dtrpS95fA2KumilN4QxtBZyqz0130_provenance.
- NP92921.RAqD0tU2MtmnC6C5EgVhbztmeFHQeLiEo-Fegs-RxoglE130_assertion description "[Evaluation of the associations between the single nucleotide polymorphisms of the promoter region of the tumor necrosis factor-alpha gene and nasopharyngeal carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92921.RAqD0tU2MtmnC6C5EgVhbztmeFHQeLiEo-Fegs-RxoglE130_provenance.
- NP92922.RAnlDtgHg0s1Vzv5NADm1k6bx4Aumb2XwFyo7vEhZyyek130_assertion description "[Investigation of functional gene polymorphisms IL-1beta, IL-6, IL-10 and TNF-alpha in individuals with recurrent aphthous stomatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92922.RAnlDtgHg0s1Vzv5NADm1k6bx4Aumb2XwFyo7vEhZyyek130_provenance.
- NP92925.RAo91lIy7ytEnvyc1d5lM1biakJySxkc2XZaShBjJs4l0130_assertion description "[Proinflammatory cytokine gene polymorphisms among Hashimoto's thyroiditis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92925.RAo91lIy7ytEnvyc1d5lM1biakJySxkc2XZaShBjJs4l0130_provenance.
- NP92929.RAgrjhPj4ApHtHYkQf11icqwTIL_0zC-dzcuSfYOIG1HE130_assertion description "[Effect of tumor necrosis factor-alpha gene polymorphism on peri-implant bone loss following prosthetic reconstruction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92929.RAgrjhPj4ApHtHYkQf11icqwTIL_0zC-dzcuSfYOIG1HE130_provenance.
- NP92930.RAtn2rjosxdkcGzHuuJBWJpCvpaO5mv0MmiZttVoLRTqg130_assertion description "[We speculate that sequence variations of important inflammatory genes of the interleukin inflammatory family are associated with differential effects in Fabry disease, and with increased sample size, haplotype blocks might be constructed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92930.RAtn2rjosxdkcGzHuuJBWJpCvpaO5mv0MmiZttVoLRTqg130_provenance.
- NP92932.RAgdyOYztJRn2TB54TWBurZPKHd7mO66_xvJmiz7tDBfc130_assertion description "[Association of tumor necrosis factor-alpha -308G>A polymorphism with IgE-mediated allergy to betalactams in an Italian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92932.RAgdyOYztJRn2TB54TWBurZPKHd7mO66_xvJmiz7tDBfc130_provenance.
- NP92938.RAmc-rAZKL9Zl2l3LYool_wbFGoNd_bY5Cz8vcPVSI4k0130_assertion description "[In this study a significantly higher level of TNF-alpha and its soluble receptors, TNF-R1 and TNF-R2, has been found in plasma of patients affected by the sporadic form of ALS compared to normal subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92938.RAmc-rAZKL9Zl2l3LYool_wbFGoNd_bY5Cz8vcPVSI4k0130_provenance.
- NP92940.RAgvQCSw7OCsaM8VucNYlJrtHbIeikiJpy22lBAmxplFM130_assertion description "[Association of TLR4 polymorphisms with symptomatic respiratory syncytial virus infection in high-risk infants and young children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92940.RAgvQCSw7OCsaM8VucNYlJrtHbIeikiJpy22lBAmxplFM130_provenance.
- NP92941.RAgaAvmqW_LNOYMemqSezxhVcmGNu-gKS1rR8FnxKxVKM130_assertion description "[Polymorphisms in Toll-like receptors-2 and -4 are not associated with disease manifestations in acute Q fever.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92941.RAgaAvmqW_LNOYMemqSezxhVcmGNu-gKS1rR8FnxKxVKM130_provenance.
- NP92944.RAgS2-ohHyZ-yGJJEMTLFJjdbU188cH4UgDF0DHWoNl9c130_assertion description "[Clinical relevance of TLR2, TLR4, CD14 and FcgammaRIIA gene polymorphisms in Streptococcus pneumoniae infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92944.RAgS2-ohHyZ-yGJJEMTLFJjdbU188cH4UgDF0DHWoNl9c130_provenance.
- NP92946.RAmRVWsdarbYlE6W2g1UatSC3GRI0zexBsq96ySUoAxlU130_assertion description "[We enrolled 250 Han Chinese in Taiwan screening for the single nucleotide polymorphisms (SNPs) in TLRs associated with viral infection, including TLR2, TLR3, TLR4, TLR7, TLR8, and TLR9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92946.RAmRVWsdarbYlE6W2g1UatSC3GRI0zexBsq96ySUoAxlU130_provenance.
- NP92950.RAqFq_SIoQK3kmYxsXbUktZMtV_TCmnsQy5FGN5BwnRWs130_assertion description "[We enrolled 250 Han Chinese in Taiwan screening for the single nucleotide polymorphisms (SNPs) in TLRs associated with viral infection, including TLR2, TLR3, TLR4, TLR7, TLR8, and TLR9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92950.RAqFq_SIoQK3kmYxsXbUktZMtV_TCmnsQy5FGN5BwnRWs130_provenance.
- NP92953.RAotLe9MVR4P1FGaNrAIJeIrsmvkZrWjvYdTVjFfAo6ms130_assertion description "[Association of polymorphisms of the MMP-2 and TIMP-2 genes with the risk of endometriosis in North Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92953.RAotLe9MVR4P1FGaNrAIJeIrsmvkZrWjvYdTVjFfAo6ms130_provenance.
- NP92956.RAtuiyaXE3D7egpim1w88vnI5Ax04A7qcc0HqPWXFHb1Q130_assertion description "[A role of thrombospondins (TSPs) in atherosclerosis and thrombosis was suggested by associations of single nucleotide polymorphisms in the genes coding for TSP-1 (rs2228262; Asn700Ser), TSP-2 (rs8089; 3' untranslated region), and TSP-4 (rs1866389; Ala387Pro) with myocardial infarction (MI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92956.RAtuiyaXE3D7egpim1w88vnI5Ax04A7qcc0HqPWXFHb1Q130_provenance.
- NP92960.RAoLq-Dqj_eEeQlgPqK3hvzQ9-y1bkFb4nInQ6kcywemo130_assertion description "[reduced TG2 activity can contribute to disorders of glucose metabolism possibly via an impairment of insulin secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92960.RAoLq-Dqj_eEeQlgPqK3hvzQ9-y1bkFb4nInQ6kcywemo130_provenance.
- NP92970.RAokJ7rC35iK-SEPeEP1x3hD2_SiMWNz3udoCzC1AfwfI130_assertion description "[The promoter region (-800, -509) polymorphisms of transforming growth factor-beta1 (TGF-beta1) gene and recurrent spontaneous abortion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92970.RAokJ7rC35iK-SEPeEP1x3hD2_SiMWNz3udoCzC1AfwfI130_provenance.
- NP92971.RAk0wxKjUGOJ0VT1HB3WQFpFwnZVl0bAfjCASWD-WTnv0130_assertion description "[TNF-alpha-308A allele, a possible severity risk factor of hemorrhagic manifestation in dengue fever patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92971.RAk0wxKjUGOJ0VT1HB3WQFpFwnZVl0bAfjCASWD-WTnv0130_provenance.
- NP92977.RAhSJj9wh_xRHJNfKGn46HdYdYC6xUOWQ3vt3wIYbVkQM130_assertion description "[Cytokine single nucleotide polymorphisms in Iranian patients with pulmonary tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92977.RAhSJj9wh_xRHJNfKGn46HdYdYC6xUOWQ3vt3wIYbVkQM130_provenance.
- NP92986.RAn-mQ3hJTbykmKqxN131b6RgrmeXxYkOXJB5JKnsWc5Q130_assertion description "[In contrast to previous allelic association studies, neither of the polymorphisms has been associated with the outcome of kidney transplantation in the single locus analysis nor in the haplotype model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92986.RAn-mQ3hJTbykmKqxN131b6RgrmeXxYkOXJB5JKnsWc5Q130_provenance.
- NP92989.RAuMd5Gifp-8O_UiBq4hpmEXD3VQfY4BEToZadPyDaSrs130_assertion description "[Determination of TGFB1 SNPs allele frequencies in different ethnic groups is useful for both population genetic analyses and association studies with immunological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92989.RAuMd5Gifp-8O_UiBq4hpmEXD3VQfY4BEToZadPyDaSrs130_provenance.
- NP92997.RAjeAakDAjU8wrPC4J_KI4CIG87WQuoSXzAXgr50_l7dM130_assertion description "[Polymorphisms in metabolic genes, their combination and interaction with tobacco smoke and alcohol consumption and risk of gastric cancer: a case-control study in an Italian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92997.RAjeAakDAjU8wrPC4J_KI4CIG87WQuoSXzAXgr50_l7dM130_provenance.
- NP92998.RAs_6y3eZYe93zFPjVjzGRvLYBMGquNPJIRWPb0vNXjBw130_assertion description "[This is the first report on the combined association of CYP1A1 and SULT gene polymorphisms in endometrial cancer that suggests a decreased single nucleotide polymorphism of CYP1A1 and an increased single nucleotide polymorphism for SULT1A1 and SULT1E1 genes may be risk factors for endometrial cancer in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92998.RAs_6y3eZYe93zFPjVjzGRvLYBMGquNPJIRWPb0vNXjBw130_provenance.
- NP93001.RAjGbl1VqNwcsIFrFsl8TkEri6KwBXVtpJAfN7-jWG834130_assertion description "[In this study, we investigated whether genetic variation in the JAK2 gene and the STAT gene region (STAT3, STAT5A and STAT5B) is associated with breast cancer (BC) risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93001.RAjGbl1VqNwcsIFrFsl8TkEri6KwBXVtpJAfN7-jWG834130_provenance.
- NP93007.RAqLNkhot_Rqs-OfguRXiqo0TYLs0F0R8V9KCmsY7ObXU130_assertion description "[Screening of the SPTBN2 (SCA5) gene in German SCA patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93007.RAqLNkhot_Rqs-OfguRXiqo0TYLs0F0R8V9KCmsY7ObXU130_provenance.
- NP93011.RAjx-gXFxMTvIAOdc-5NKQKerCHd34j2ZgY9j1btrXRLs130_assertion description "[Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93011.RAjx-gXFxMTvIAOdc-5NKQKerCHd34j2ZgY9j1btrXRLs130_provenance.
- NP93012.RAtVGSqqH8yCzsZkqdEgs5TClNJNHuQiInTZRE88N9_mc130_assertion description "[Manganese superoxide dismutase (Mn-SOD) gene polymorphisms in urolithiasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93012.RAtVGSqqH8yCzsZkqdEgs5TClNJNHuQiInTZRE88N9_mc130_provenance.
- NP93023.RAt1yMnOpXCmw-6V-B3rttkFpLxt6yTbG0Jq9Na2vayuM130_assertion description "[Association of the dopamine transporter gene and ADHD symptoms in a Canadian population-based sample of same-age twins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93023.RAt1yMnOpXCmw-6V-B3rttkFpLxt6yTbG0Jq9Na2vayuM130_provenance.
- NP93026.RAunJK6M32J2HbgUp1EMiZRr9FjLKG14Wyqjr5ycrMgyc130_assertion description "[HPA axis reactivity: a mechanism underlying the associations among 5-HTTLPR, stress, and depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93026.RAunJK6M32J2HbgUp1EMiZRr9FjLKG14Wyqjr5ycrMgyc130_provenance.
- NP93028.RAvKJk4FUhoEggYu9oyNfKqSEdacDKndyBZo9G4GfjK7Q130_assertion description "[Mutagen sensitivity of peripheral blood from women carrying a BRCA1 or BRCA2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93028.RAvKJk4FUhoEggYu9oyNfKqSEdacDKndyBZo9G4GfjK7Q130_provenance.
- NP93033.RAjCZ4R2Hu0BkSlC5VJBG2Hx4CcrJjSdGbnFIVI2f9N3c130_assertion description "[Integrated pharmacogenetic prediction of irinotecan pharmacokinetics and toxicity in patients with advanced non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93033.RAjCZ4R2Hu0BkSlC5VJBG2Hx4CcrJjSdGbnFIVI2f9N3c130_provenance.
- NP93034.RAl4XF7SlWTNKEebgWg7zM9tHXzGK-qPvtrWFNKMY5VTQ130_assertion description "[Influence of the organic anion-transporting polypeptide 1B1 (OATP1B1) polymorphisms on irinotecan-pharmacokinetics and clinical outcome of patients with advanced non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93034.RAl4XF7SlWTNKEebgWg7zM9tHXzGK-qPvtrWFNKMY5VTQ130_provenance.
- NP93036.RAk2DMZI7S53dF4_STWiz3al0Qzt7A9Nc2TXXE-6z3kEE130_assertion description "[Variation in the NRAMP1 gene does not affect susceptibility or protection in human brucellosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93036.RAk2DMZI7S53dF4_STWiz3al0Qzt7A9Nc2TXXE-6z3kEE130_provenance.
- NP93044.RAgB8wnVntLVdB27kVFzOaHFccfowF8HZF0TL_SorRIYw130_assertion description "[Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93044.RAgB8wnVntLVdB27kVFzOaHFccfowF8HZF0TL_SorRIYw130_provenance.
- NP93049.RAlMKpbwaYryL2A8iZSNehIg3_VjjE-iu7HEbzKta_gDg130_assertion description "[The importance of expression of interferon gamma-inducible protein of 10 kilodaltons (IP-10, CXCL10) during chronic hepatitis B virus (HBV) infection has been recently emphasized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93049.RAlMKpbwaYryL2A8iZSNehIg3_VjjE-iu7HEbzKta_gDg130_provenance.
- NP93051.RAr311XRrgeLTf2WzrbxiotiT91Uj1wsXmYkdjJrw57js130_assertion description "[Association between RANTES functional polymorphisms and tuberculosis in Hong Kong Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93051.RAr311XRrgeLTf2WzrbxiotiT91Uj1wsXmYkdjJrw57js130_provenance.
- NP93052.RAl4lAW5j84DBPtSiJXvAQ2_Z5Z_9beWrvfJG-mB_eeJs130_assertion description "[In contrast to previous allelic association studies, neither of the polymorphisms has been associated with the outcome of kidney transplantation in the single locus analysis nor in the haplotype model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93052.RAl4lAW5j84DBPtSiJXvAQ2_Z5Z_9beWrvfJG-mB_eeJs130_provenance.
- NP93067.RAuuSrPTLdGpIior--4hxh4ejl1vRppT_x5EHe5zJTi34130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93067.RAuuSrPTLdGpIior--4hxh4ejl1vRppT_x5EHe5zJTi34130_provenance.
- NP93090.RAuCYVf8dz7K8njlCO2f6AK4bLqxgTGJxF5rM9N_zOy8Q130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93090.RAuCYVf8dz7K8njlCO2f6AK4bLqxgTGJxF5rM9N_zOy8Q130_provenance.
- NP93092.RAnQAc_Eft9_cxDr-Ro-4DNeT5LMNGfkn441ueug8F36g130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93092.RAnQAc_Eft9_cxDr-Ro-4DNeT5LMNGfkn441ueug8F36g130_provenance.
- NP93094.RApA04EIz30pHQ-52dWeauknPjwSPoCGf872KHY9dR1RE130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93094.RApA04EIz30pHQ-52dWeauknPjwSPoCGf872KHY9dR1RE130_provenance.
- NP93095.RAodSTlfNC2C6iATPsQjrZSW6Jvuu0choUlV7YC1bvU9Y130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93095.RAodSTlfNC2C6iATPsQjrZSW6Jvuu0choUlV7YC1bvU9Y130_provenance.